{{Rsnum
|rsid=397514656
|Chromosome=5
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MEF2C
|position=88804776
|Gene_s=MEF2C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=5
|CLNACC=RCV000033231.2
|CLNALLE=1
|CLNDBN=Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3150700:613443:228384
|CLNHGVS=NC_000005.9:g.88100593C>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600662.0004
|Disease=Mental retardation
|FwdALT=C
|FwdREF=G
|GENEINFO=MEF2C:4208
|GENE_ID=4208
|GENE_NAME=MEF2C
|REF=C
|RSPOS=88100593
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514656
}}